ReviewPharmacoEconomics2026
Waiting for Trial Evidence or Using Real-World Evidence: Trade-Offs for Coverage with Evidence Development.
Review in PharmacoEconomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Coverage with evidence development (CED) is used to manage uncertainty in new health technologies, but its implementation varies across settings. Some evidence-development arrangements restrict access to patients participating in randomized controlled trials (RCTs), whereas others provide broader conditional coverage while real-world evidence (RWE) is generated concurrently. RWE may be generated more quickly than trial evidence, often using larger samples and at lower cost. However, it is vulnerable to bias such as unmeasured confounding, and both the magnitude and direction of such bias are typically unknown. Decision-makers therefore lack an ex ante framework for determining when RWE-based CED is preferable to RCT-based CED. We develop a decision-analytic framework that extends value-of-information methods by incorporating an explicit bias parameter to capture structural distortion in RWE treatment effect estimates. Drawing on quantitative bias analysis, the framework defines policy indifference bias thresholds as the primary decision metric, identifying the maximum tolerable bias for RWE-based CED to remain preferred. The framework also quantifies, as a complementary measure, the probability of RCT-based CED dominance, defined as the ex ante probability that the RCT-based strategy is more favorable even when RWE is unbiased. A case study illustrates how these two metrics are determined.
Identifiers
42853373What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.